NDC 68180-348-01 - Gabapentin

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 68180-348
Requested NDC: 68180-348-01
Package NDCs from labels: 68180-348-01, 68180-348-02
Manufacturer: Lupin Pharmaceuticals, Inc. | LUPIN LIMITED
Effective date: 2018-09-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Gabapentin - Lupin Pharmaceuticals, Inc. \| LUPIN LIMITED	Lupin Pharmaceuticals, Inc. \| LUPIN LIMITED	2018-09-04	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68180-348-01	Gabapentin	100 in 1 BOTTLE	TABLET, FILM COATED	100		7
68180-348-02	Gabapentin	500 in 1 BOTTLE	TABLET, FILM COATED	500		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68180-348	GABAPENTIN TABLET, FILM COATED [LUPIN PHARMACEUTICALS, INC.]	7	2 package rows	20180905_d53b9838-f47a-40df-bf6d-71e7166b6101.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 21 of 21 · 401 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Gabapentin	GABAPENTIN	Bi-Coastal Pharma International LLC	e0cd96d1-b1ef-46ec-a5a3-9505b0811b8b	2016-04-17	Warnings, Adverse reactions	Exact identifier unii: 6CW7F3G59X

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.